HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2062250Generated: October 31, 2026
Sodium Hydroxide → 2-(2-((tert-Butoxycarbonyl)(methyl)amino)-N-methylacetamido)acetic acid
https://huagongshe.com/reaction/2062250
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | {[2-(Tert-butoxycarbonyl-methyl-amino)acetyl]-methyl-amino}-acetic acid ethyl ester | HCID 57470192 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(2-((tert-Butoxycarbonyl)(methyl)amino)-N-methylacetamido)acetic acid | HCID 51358234 | — |
Reaction Steps
The ester was taken up in 49 mL of methanol, and to this was added a 1 M NaOH solution (25.1 mL, 25 mmol). The reaction mixture was heated at 65° C. for 3 h. The reaction mixture was cooled, and methanol was removed under reduced pressure. The residue was diluted with 50 mL of water and acidified with glacial acetic acid until the pH was 5. This solution was extracted with EtOAc (50 mL), and the organic layer was separated and dried over Na2SO4, and the solvent was removed under reduced pressure to give {[2-(tert-Butoxycarbonyl-methyl-amino)-acetyl]-methyl-amino}-acetic acid as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08283354B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-0a5c606821ce4e25b9a48b86855c26ee |
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| Source note | uspto-grants-2012_10 |
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